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FDA Cosmetic registration is an FDA post-market reporting system for use by manufacturers,
packers, and distributors of cosmetic products that are in commercial distribution in the US. There are
two parts in FDA Voluntary Cosmetic Registration Program. Voluntary Cosmetic Establishments
Registration and Cosmetic Product Ingredient Statements (CPIS) Filing.
The State of California has imposed additional requirements for cosmetic products intended for use in
California.
Qpro Regulatory Services are always happy to assist you. Complete the following questionnaire which
is self explanatory. Please feel free to contact us if you have any queries.
FDA VOLUNTARY COSMETIC REGISTRATION PROGRAM
U.S. FDA Voluntary Cosmetic Registration Program is Post-market reporting system. A company can
participate in Voluntary Cosmetic Registration Program only if their products are in commercial
distribution in USA.
Date: _ _ - _ _ - 201_
Signature
qproregulatoryservices@gmail.com
www.usfdacosmetics.net
Amendment
Cancellation
Business Type:
Manufacturer
Packer
Both
Others: ______________________
Middle Name
Last Name
qproregulatoryservices@gmail.com
www.usfdacosmetics.net
DOING BUSINESS AS
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PAYMENT INFORMATION
PayPal Transaction Number (ID): ___________________________________________________
Date of Payment: _ _ - _ _ - 201__
{Please contact us for Payment related queries or any other information. We are always happy to assist you.}
qproregulatoryservices@gmail.com
www.usfdacosmetics.net
AGREEMENT
Qpro Regulatory Services and the undersigned party have today entered into an agreement
regarding the provision of consultancy services on the terms and conditions laid out in this
Agreement.
In rendering consulting services under this Agreement, Qpro Regulatory Services shall conform
to standards of work and business ethics. However, Qpro Regulatory Services shall bear no
liability or otherwise be responsible for complete assurance and delays in the provision of
Services.
The Client agrees to provide accurate and sufficient information, adequate technical assistance
and documentation, required for Qpro Regulatory Services to be able to perform the Services.
The Client shall promptly provide further information Qpro Regulatory Services reasonably
deems relevant to perform the task.
The Client is solely responsible for the scientific accuracy, material facts and completeness of
information provided to Qpro Regulatory Services.
The Client shall pay to Qpro Regulatory Services fees at the rate specified in the Purchase
Order.
The Parties agree to make all reasonable efforts, in good faith, to resolve any dispute arising
from implementation of this agreement through informal discussions and the development of
mutual satisfactory options.
Qpro Regulatory Services liability in whatever kind or nature cannot exceed the fee for
performing the task.
This Agreement shall terminate automatically upon completion by Qpro Regulatory Services of
the Services required by this Agreement or 30 calendar days from the effective date of this
agreement.
Qpro Regulatory Services is a Private business entity and is not affiliated with U.S. FDA.
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qproregulatoryservices@gmail.com
www.usfdacosmetics.net